PRIDE-study.
Recruiting
- Conditions
- focal liver lesions
- Registration Number
- NL-OMON24607
- Lead Sponsor
- Dr. R. van Hillegersberg, SurgeonCoordinating Investigator/Project leader/Principal Investigator:University Medical Center UtrechtHeidelberglaan 100, 3584 CX Utrecht,The Netherlands
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 230
Inclusion Criteria
1. Age > 18 years;
2. Suspicion of focal liver lesions, both benign and/or malignant:
Exclusion Criteria
1. Clinical query on liver MRI chart directed to other liver disease than focal liver lesions like liver cirrhosis, hepatitis, or liver abscess (these are no exclusion criteria when apparent as secondary disease to focal disease);
2. Previous liver surgery;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the diagnostic value of MR-Primovist and Respiratory Triggered DWI MRI for the detection and characterization of focal liver lesions.<br>
- Secondary Outcome Measures
Name Time Method 1. Accuracy and agreement between MR-Gadovist and MR-Primovist for lesion detection and characterization on a per lesion basis;<br /><br>2. Change in surgical strategy.